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Gene-Drug Interaction in Stroke

机译:脑卒中的基因药物相互作用

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Stroke is the third cause of mortality and one of most frequent causes of long-term neurological disability, as well as a complex disease that results from the interaction of environmental and genetic factors. The focus on genetics has produced a large number of studies with the objective of revealing the genetic basis of cerebrovascular diseases. Furthermore, pharmacogenetic research has investigated the relation between genetic variability and drug effectiveness/toxicity. This review will examine the implications of pharmacogenetics of stroke; data on antihypertensives, statins, antiplatelets, anticoagulants, and recombinant tissue plasminogen activator will be illustrated. Several polymorphisms have been studied and some have been associated with positive drug-gene interaction on stroke, but the superiority of the genotype-guided approach over the clinical approach has not been proved yet; for this reason, it is not routinely recommended.
机译:中风是导致死亡的第三大原因,也是长期神经系统残疾的最常见原因之一,也是由环境因素和遗传因素共同作用导致的复杂疾病。对遗传学的关注已进行了大量研究,目的是揭示脑血管疾病的遗传基础。此外,药物遗传学研究已经研究了遗传变异性与药物有效性/毒性之间的关系。这篇综述将研究中风的药理遗传学意义。将说明有关降压药,他汀类药物,抗血小板药,抗凝剂和重组组织纤溶酶原激活剂的数据。已经研究了几种多态性,有些与卒中中药物基因的正向相互作用有关,但是尚未证明基因型指导的方法优于临床方法。因此,通常不建议使用。

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